BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    POWERPACK

    FDA Adverse Event
    Malfunction ·ICC-NEXERGY·Product code IYN·September 3, 2013

    DORMA 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 16, 2022

    BD PHASEAL PROTECTOR P50J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 7, 2023

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·May 24, 2013

    12/14 ARTICUL 44MM M SPEC+5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·September 30, 2014

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·June 16, 2011